We have developed a unique portfolio of consumables, each adapted to the different feed water quality requirements and to your various applications. To maintain your water system’s performance, it’s critical to replace your purification cartridges on time and with genuine ISO 9001-certified parts.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Female Luer Lok
Length
3.9 cm (1.52 in.)
Material Size
6
Maximum Inlet Pressure, bar (psi)
4.0 bar (60 psi) @ 25 °C
Media
Multimedia Durapore®
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Outlet Connection
Male Luer Lok
Pore Size
1.2 / 0.5 / 0.22 µm
Sterility
Other
Sterilization
1 autoclave cycle of 60 min @ 123 °C
Support Material
Polypropylene
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Female Luer Lok
Length
3.9 cm (1.52 in.)
Material Size
6
Maximum Inlet Pressure, bar (psi)
4.0 bar (60 psi) @ 25 °C
Media
Multimedia Durapore®
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Outlet Connection
Male Luer Lok
Pore Size
0.5 / 0.2 / 0.22 µm
Sterility
Other
Sterilization
1 autoclave cycle of 60 min @ 123 °C
Support Material
Polypropylene
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Female Luer Lok
Length
3.9 cm (1.52 in.)
Material Size
6
Maximum Inlet Pressure, bar (psi)
4.0 bar (60 psi) @ 25 °C
Media
Multimedia Durapore®
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Outlet Connection
Male Luer Lok
Pore Size
0.5 / 0.2 / 0.22 µm
Sterility
Other
Sterilization
1 autoclave cycle of 60 min @ 123 °C
Support Material
Polypropylene
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Female Luer Lok
Length
3.9 cm (1.52 in.)
Material Size
6
Maximum Inlet Pressure, bar (psi)
4.0 bar (60 psi) @ 25 °C
Media
Multimedia Durapore®
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Outlet Connection
Male Luer Lok
Pore Size
1.2 / 0.2 / 0.22 µm
Sterility
Other
Sterilization
1 autoclave cycle of 60 min @ 123 °C
Support Material
Polypropylene
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.
Inlet Connection
Female Luer Lok
Length
3.9 cm (1.52 in.)
Material Size
6
Maximum Inlet Pressure, bar (psi)
4.0 bar (60 psi) @ 25 °C
Media
Multimedia Durapore®
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Outlet Connection
Male Luer Lok
Pore Size
1.2 / 0.2 / 0.22 µm
Sterility
Other
Sterilization
1 autoclave cycle of 60 min @ 123 °C
Support Material
Polypropylene
Trade Name
OptiScale®
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.25 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Code
Code 0 (2-222) O-rings
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
CW0301SB1
Chemistry
Mixed Cellulose Esters (MCE)
Device Configuration
Cartridge
Device Material
Polypropylene
Device Size
10 in.
Diameter
7.1 cm (2.8 in.)
Filter Grade
Standard Milligard® Media
Filtration Area
0.8 m²
Format
Single Layer
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Gravimetric Extractables
The extractables level was equal to or less than 50 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
10 in. (25 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
3.5 bar (50 psid) @ 25 °C
Maximum Inlet Pressure, bar (psi)
3.5 bar (50 psi) @ 25 °C
Media
Maximum Differential Pressure, bar (psid)
Nominal Pore Size
0.2 µm
Non-Fiber Releasing
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Code
Code 0 (2-222) O-rings
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
CW0301SB1
Chemistry
Mixed Cellulose Esters (MCE)
Device Configuration
Cartridge
Device Material
Polypropylene
Device Size
10 in.
Diameter
7.1 cm (2.8 in.)
Filter Grade
Standard Milligard® Media
Filtration Area
0.8 m²
Format
Single Layer
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Gravimetric Extractables
The extractables level was equal to or less than 50 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
10 in. (25 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
3.5 bar (50 psid) @ 25 °C
Maximum Inlet Pressure, bar (psi)
3.5 bar (50 psi) @ 25 °C
Media
Maximum Differential Pressure, bar (psid)
Nominal Pore Size
0.2 µm
Non-Fiber Releasing
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Cartridge Code
Code 0 (2-222) O-rings
Cartridge Nominal Length
10 in. (25 cm)
Catalogue Number
CW0601SB1
Chemistry
Mixed Cellulose Esters (MCE)
Device Configuration
Cartridge
Device Material
Polypropylene
Device Size
10 in.
Diameter
7.1 cm (2.8 in.)
Filter Grade
Standard Milligard® Media
Filtration Area
0.8 m²
Format
Single Layer
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Gravimetric Extractables
The extractables level was equal to or less than 50 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
Key Applications
Food and BeverageBeerBottled WaterWine
Length
10 in. (25 cm)
Material Package
Double Easy-Open bag
Material Size
1
Maximum Differential Pressure, bar (psid)
3.5 bar (50 psid) @ 25 °C
Maximum Inlet Pressure, bar (psi)
3.5 bar (50 psi) @ 25 °C
Media
Maximum Differential Pressure, bar (psid)
Nominal Pore Size
0.5 µm
Non-Fiber Releasing
This product was manufactured with a media combination which meets the criteria for a "non-fiber releasing" filter as defined in 21 CFR 210.3 (b) (6).
Trust Merck membrane filtration devices for the collection and preparation of samples, mobile phases, and buffers to obtain the highest quality results from downstream analysis.
Whether you need to collect, separate, or remove contaminants from air or fluid samples prior to downstream analysis, our broad selection of syringe filters, membranes, filter holders and related filtration devices ensures that we have the right solution for your application.
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